FDA 510(k)

ALLIANCE RUBBER, EC-GRIP

K-Number: K972801 · 1997-10-21

ApplicantAlliance Rubber Products Sdn. Bhd.

Decision Date1997-10-21

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ALLIANCE RUBBER, EC-GRIP is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Rubber Products Sdn. Bhd.. It received FDA 510(k) clearance on 1997-10-21 under 510(k) number K972801. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLIANCE RUBBER, EC-GRIP?

ALLIANCE RUBBER, EC-GRIP is a medical device that received FDA 510(k) clearance on 1997-10-21. The listed applicant is Alliance Rubber Products Sdn. Bhd.. The 510(k) number is K972801.

When did ALLIANCE RUBBER, EC-GRIP receive FDA 510(k) clearance?

ALLIANCE RUBBER, EC-GRIP received FDA 510(k) clearance on 1997-10-21, under 510(k) number K972801.

Who is the listed applicant for ALLIANCE RUBBER, EC-GRIP?

The FDA 510(k) record lists Alliance Rubber Products Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLIANCE RUBBER, EC-GRIP?

The FDA product code for ALLIANCE RUBBER, EC-GRIP is LYY.

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Other records listing Alliance Rubber Products Sdn. Bhd. as applicant

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Related Devices (Code: LYY)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.